<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/11609?offset=710</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/30867/perl-special-vars-quick-reference</guid>
	<pubDate>Tue, 07 Feb 2017 05:08:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/30867/perl-special-vars-quick-reference</link>
	<title><![CDATA[Perl Special Vars Quick Reference]]></title>
	<description><![CDATA[<table>
<tbody>
<tr>
<td><tt>$_</tt></td>
<td>The default or implicit variable.</td>
</tr>
<tr>
<td><tt>@_</tt></td>
<td>Subroutine parameters.</td>
</tr>
<tr>
<td><tt>$a</tt><br /><tt>$b</tt></td>
<td><a href="http://perldoc.perl.org/functions/sort.html">sort</a>&nbsp;comparison routine variables.</td>
</tr>
<tr>
<td><tt>@ARGV</tt></td>
<td>The command-line args.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Regular Expressions</span></td>
</tr>
<tr>
<td><tt>$&lt;digit&gt;</tt></td>
<td>Regexp parenthetical capture holders.</td>
</tr>
<tr>
<td><tt>$&amp;</tt></td>
<td>Last successful match (degrades performance).</td>
</tr>
<tr>
<td><tt>${^MATCH}</tt></td>
<td>Similar to&nbsp;<tt>$&amp;</tt>&nbsp;without performance penalty. Requires /p modifier.</td>
</tr>
<tr>
<td><tt>$`</tt></td>
<td>Prematch for last successful match string (degrades performance).</td>
</tr>
<tr>
<td><tt>${^PREMATCH}</tt></td>
<td>Similar to&nbsp;<tt>$`</tt>&nbsp;without performance penalty. Requires&nbsp;<tt>/p</tt>&nbsp;modifier.</td>
</tr>
<tr>
<td><tt>$'</tt></td>
<td>Postmatch for last successful match string (degrades performance).</td>
</tr>
<tr>
<td><tt>${^POSTMATCH}</tt></td>
<td>Similar to&nbsp;<tt>$'</tt>&nbsp;without performance penalty. Requires&nbsp;<tt>/p</tt>&nbsp;modifier.</td>
</tr>
<tr>
<td><tt>$+</tt></td>
<td>Last paren match.</td>
</tr>
<tr>
<td><tt>$^N</tt></td>
<td>Last closed paren match (last submatch).</td>
</tr>
<tr>
<td><tt>@+</tt></td>
<td>Offsets of ends of successful submatches in scope.</td>
</tr>
<tr>
<td><tt>@-</tt></td>
<td>Offsets of starts of successful submatches in scope.</td>
</tr>
<tr>
<td><tt>%+</tt></td>
<td>Like&nbsp;<tt>@+</tt>, but for named submatches.</td>
</tr>
<tr>
<td><tt>%-</tt></td>
<td>Like&nbsp;<tt>@-</tt>, but for named submatches.</td>
</tr>
<tr>
<td><tt>$^R</tt></td>
<td>Last regexp (?{code}) result.</td>
</tr>
<tr>
<td><tt>${^RE_DEBUG_FLAGS}</tt></td>
<td>Current value of regexp debugging flags. See&nbsp;<tt>use re 'debug';</tt></td>
</tr>
<tr>
<td><tt>${^RE_TRIE_MAXBUF}</tt></td>
<td>Control memory allocations for RE optimizations for large alternations.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Encoding</span></td>
</tr>
<tr>
<td><tt>${^ENCODING}</tt></td>
<td>The object reference to the Encode object, used to convert the source code to Unicode.</td>
</tr>
<tr>
<td><tt>${^OPEN}</tt></td>
<td>Internal use: \0 separated Input / Output layer information.</td>
</tr>
<tr>
<td><tt>${^UNICODE}</tt></td>
<td>Read-only Unicode settings.</td>
</tr>
<tr>
<td><tt>${^UTF8CACHE}</tt></td>
<td>State of the internal UTF-8 offset caching code.</td>
</tr>
<tr>
<td><tt>${^UTF8LOCALE}</tt></td>
<td>Indicates whether UTF8 locale was detected at startup.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">IO and Separators</span></td>
</tr>
<tr>
<td><tt>$.</tt></td>
<td>Current line number (or record number) of most recent filehandle.</td>
</tr>
<tr>
<td><tt>$/</tt></td>
<td>Input record separator.</td>
</tr>
<tr>
<td><tt>$|</tt></td>
<td>Output autoflush. 1=autoflush, 0=default. Applies to currently selected handle.</td>
</tr>
<tr>
<td><tt>$,</tt></td>
<td>Output field separator (lists)</td>
</tr>
<tr>
<td><tt>$\</tt></td>
<td>Output record separator.</td>
</tr>
<tr>
<td><tt>$"</tt></td>
<td>Output list separator. (interpolated lists)</td>
</tr>
<tr>
<td><tt>$;</tt></td>
<td>Subscript separator. (Use a real multidimensional array instead.)</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Formats</span></td>
</tr>
<tr>
<td><tt>$%</tt></td>
<td>Page number for currently selected output channel.</td>
</tr>
<tr>
<td><tt>$=</tt></td>
<td>Current page length.</td>
</tr>
<tr>
<td><tt>$-</tt></td>
<td>Number of lines left on page.</td>
</tr>
<tr>
<td><tt>$~</tt></td>
<td>Format name.</td>
</tr>
<tr>
<td><tt>$^</tt></td>
<td>Name of top-of-page format.</td>
</tr>
<tr>
<td><tt>$:</tt></td>
<td>Format line break characters</td>
</tr>
<tr>
<td><tt>$^L</tt></td>
<td>Form feed (default "\f").</td>
</tr>
<tr>
<td><tt>$^A</tt></td>
<td>Format Accumulator</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Status Reporting</span></td>
</tr>
<tr>
<td><tt>$?</tt></td>
<td>Child error. Status code of most recent system call or pipe.</td>
</tr>
<tr>
<td><tt>$!</tt></td>
<td>Operating System Error. (What just went 'bang'?)</td>
</tr>
<tr>
<td><tt>%!</tt></td>
<td>Error number hash</td>
</tr>
<tr>
<td><tt>$^E</tt></td>
<td>Extended Operating System Error (Extra error explanation).</td>
</tr>
<tr>
<td><tt>$@</tt></td>
<td>Eval error.</td>
</tr>
<tr>
<td><tt>${^CHILD_ERROR_NATIVE}</tt></td>
<td>Native status returned by the last pipe close, backtick (`` ) command, successful call to wait() or waitpid(), or from the system() operator.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">ID's and Process Information</span></td>
</tr>
<tr>
<td><tt>$$</tt></td>
<td>Process ID</td>
</tr>
<tr>
<td><tt>$&lt;</tt></td>
<td>Real user id of process.</td>
</tr>
<tr>
<td><tt>$&gt;</tt></td>
<td>Effective user id of process.</td>
</tr>
<tr>
<td><tt>$(</tt></td>
<td>Real group id of process.</td>
</tr>
<tr>
<td><tt>$)</tt></td>
<td>Effective group id of process.</td>
</tr>
<tr>
<td><tt>$0</tt></td>
<td>Program name.</td>
</tr>
<tr>
<td><tt>$^O</tt></td>
<td>Operating System name.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Perl Status Info</span></td>
</tr>
<tr>
<td><tt>$]</tt></td>
<td>Old: Version and patch number of perl interpreter. Deprecated.</td>
</tr>
<tr>
<td><tt>$^C</tt></td>
<td>Current value of flag associated with&nbsp;<strong>-c</strong>&nbsp;switch.</td>
</tr>
<tr>
<td><tt>$^D</tt></td>
<td>Current value of debugging flags</td>
</tr>
<tr>
<td><tt>$^F</tt></td>
<td>Maximum system file descriptor.</td>
</tr>
<tr>
<td><tt>$^I</tt></td>
<td>Value of the&nbsp;<strong>-i</strong>&nbsp;(inplace edit) switch.</td>
</tr>
<tr>
<td><tt>$^M</tt></td>
<td>Emergency Memory pool.</td>
</tr>
<tr>
<td><tt>$^P</tt></td>
<td>Internal variable for debugging support.</td>
</tr>
<tr>
<td><tt>$^R</tt></td>
<td>Last regexp (?{code}) result.</td>
</tr>
<tr>
<td><tt>$^S</tt></td>
<td>Exceptions being caught. (eval)</td>
</tr>
<tr>
<td><tt>$^T</tt></td>
<td>Base time of program start.</td>
</tr>
<tr>
<td><tt>$^V</tt></td>
<td>Perl version.</td>
</tr>
<tr>
<td><tt>$^W</tt></td>
<td>Status of -w switch</td>
</tr>
<tr>
<td><tt>${^WARNING_BITS}</tt></td>
<td>Current set of warning checks enabled by&nbsp;<tt>use warnings;</tt></td>
</tr>
<tr>
<td><tt>$^X</tt></td>
<td>Perl executable name.</td>
</tr>
<tr>
<td><tt>${^GLOBAL_PHASE}</tt></td>
<td>Current phase of the Perl interpreter.</td>
</tr>
<tr>
<td><tt>$^H</tt></td>
<td>Internal use only: Hook into Lexical Scoping.</td>
</tr>
<tr>
<td><tt>%^H</tt></td>
<td>Internaluse only: Useful to implement scoped pragmas.</td>
</tr>
<tr>
<td><tt>${^TAINT}</tt></td>
<td>Taint mode read-only flag.</td>
</tr>
<tr>
<td><tt>${^WIN32_SLOPPY_STAT}</tt></td>
<td>If true on Windows&nbsp;<tt>stat()</tt>&nbsp;won't try to open the file.</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Command Line Args</span></td>
</tr>
<tr>
<td><tt>ARGV</tt></td>
<td>Filehandle iterates over files from command line (see also&nbsp;<tt>&lt;&gt;</tt>).</td>
</tr>
<tr>
<td><tt>$ARGV</tt></td>
<td>Name of current file when reading &lt;&gt;</td>
</tr>
<tr>
<td><tt>@ARGV</tt></td>
<td>List of command line args.</td>
</tr>
<tr>
<td><tt>ARGVOUT</tt></td>
<td>Output filehandle for -i switch</td>
</tr>
<tr>
<td colspan="2" align="center"><span style="font-size: xx-small;">Miscellaneous</span></td>
</tr>
<tr>
<td><tt>@F</tt></td>
<td>Autosplit (-a mode) recipient.</td>
</tr>
<tr>
<td><tt>@INC</tt></td>
<td>List of library paths.</td>
</tr>
<tr>
<td><tt>%INC</tt></td>
<td>Keys are filenames, values are paths to modules included via&nbsp;<tt>use, require,&nbsp;</tt>or&nbsp;<tt>do</tt>.</td>
</tr>
<tr>
<td><tt>%ENV</tt></td>
<td>Hash containing current environment variables</td>
</tr>
<tr>
<td><tt>%SIG</tt></td>
<td>Signal handlers.</td>
</tr>
<tr>
<td><tt>$[</tt></td>
<td>Array and substr first element (Deprecated!).</td>
</tr>
</tbody>
</table><p>&nbsp;</p><p>See&nbsp;<a href="http://perldoc.perl.org/perlvar.html">perlvar</a>&nbsp;for detailed descriptions of each of these (and a few more) special variables.</p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34569/ksnp30-snp-detection-and-phylogenetic-analysis-of-genomes-without-genome-alignment-or-reference-genome</guid>
	<pubDate>Fri, 08 Dec 2017 16:48:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34569/ksnp30-snp-detection-and-phylogenetic-analysis-of-genomes-without-genome-alignment-or-reference-genome</link>
	<title><![CDATA[kSNP3.0: SNP detection and phylogenetic analysis of genomes without genome alignment or reference genome]]></title>
	<description><![CDATA[<p><span>Sept. 20, 2017 Version 3.1 released. Major upgrade. Version 3.1 fixes the problems with SNP annotation that arose when NCBI discontinued use of GI numbers. Please read carefully the Preface (page 3) and the File of annotated genomes section (pages 9-10) in the version 3.1 User Guide. Thanks to Tom Slezak for revsing the get_genbank_file3 script and to Tod Stuber (USDA) for testing version 3.1 even though he doesn't need the annotation feature. All users are encouraged to upgrade to version 3.1.&nbsp;<br></span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/ksnp/files/" rel="nofollow">https://sourceforge.net/projects/ksnp/files/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36935/assemblytics-delta-file-to-analyze-alignments-of-an-assembly-to-another-assembly-or-a-reference-genome</guid>
	<pubDate>Thu, 14 Jun 2018 07:31:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36935/assemblytics-delta-file-to-analyze-alignments-of-an-assembly-to-another-assembly-or-a-reference-genome</link>
	<title><![CDATA[assemblytics: delta file to analyze alignments of an assembly to another assembly or a reference genome]]></title>
	<description><![CDATA[Download and install MUMmer
Align your assembly to a reference genome using nucmer (from MUMmer package)
$ nucmer -maxmatch -l 100 -c 500 REFERENCE.fa ASSEMBLY.fa -prefix OUT
Consult the MUMmer manual if you encounter problems

Optional: Gzip the delta file to speed up upload (usually 2-4X faster)
$ gzip OUT.delta
Then use the OUT.delta.gz file for upload.
Upload the .delta or delta.gz file (view example) to Assemblytics
Important: Use only contigs rather than scaffolds from the assembly. This will prevent false positives when the number of Ns in the scaffolded sequence does not match perfectly to the distance in the reference.

The unique sequence length required represents an anchor for determining if a sequence is unique enough to safely call variants from, which is an alternative to the mapping quality filter for read alignment.

http://assemblytics.com/<p>Address of the bookmark: <a href="http://assemblytics.com/" rel="nofollow">http://assemblytics.com/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/41230/curated-set-of-ribosomal-rna-rrna-reference-sequences-targeted-loci-with-verifiable-organism</guid>
	<pubDate>Sun, 23 Feb 2020 02:17:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/41230/curated-set-of-ribosomal-rna-rrna-reference-sequences-targeted-loci-with-verifiable-organism</link>
	<title><![CDATA[Curated set of ribosomal RNA (rRNA) reference sequences (targeted loci) with verifiable organism]]></title>
	<description><![CDATA[<p>MCBI have a curated set of ribosomal RNA (rRNA) reference sequences (targeted loci) with verifiable organism sources and current names. This set is critical for correctly identifying and classifying prokaryotic (bacteria and archaea) and fungal samples. To provide easy access to these sequences, we recently added a separate rRNA/ITS databases section on the nucleotide BLAST page for these targeted sequences that makes it convenient to quickly identify source organisms. The new databases are: </p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *16S ribosomal RNA (Bacteria and Archaea)</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *18S ribosomal RNA sequences (SSU) from Fungi type and reference material&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *28S ribosomal RNA sequences (LSU) from Fungi type and reference material</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *Internal transcribed spacer region (ITS) from Fungi type and reference material</p><p>You can also download these from the BLAST db FTP area.&nbsp; See the <a href="https://go.usa.gov/xdEBX" target="_blank">NCBI Insights post</a> for more detail. </p><p>Useful links</p><p>-----------------</p><p><a href="https://go.usa.gov/xdEj5" target="_blank">BLAST form with rRNA/ITS databases</a></p><p><a href="https://ftp.ncbi.nlm.nih.gov/blast/db/" target="_blank">BLAST db download</a></p><p><a href="https://www.ncbi.nlm.nih.gov/refseq/targetedloci/" target="_blank">Targeted loci</a></p><p><span style="color: black;">If you have any questions or concerns, please contact <a href="mailto:blast-help@ncbi.nlm.nih.gov" target="_blank" title="Follow link">blast-help@ncbi.nlm.nih.gov<sup><span style="color: black; text-decoration: none;"><img src="https://mail.google.com/mail/u/0?ui=2&amp;ik=024a8aa0b9&amp;attid=0.1&amp;permmsgid=msg-f:1659255165855446848&amp;th=1706dbc8408bb740&amp;view=fimg&amp;sz=s0-l75-ft&amp;attbid=ANGjdJ_drW2ArYDNLoHrQh36gm6rp2Std8ZUSplCzP6bYQSQYBsQfZ_85vOujXOdTRdaLxrR7QeEBVUbyACPBJHhFUeIglX8G7Ew7TcclzhvO7fJhiz7sIdkkDgZ7QA&amp;disp=emb" alt="https://jira.ncbi.nlm.nih.gov/images/icons/mail_small.gif" width="13" height="12" style="border: 0px;"></span></sup></a></span></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/12111/internship-program-with-arraygen-technolgies</guid>
  <pubDate>Sun, 22 Jun 2014 23:18:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Internship program with ArrayGen Technolgies]]></title>
  <description><![CDATA[
<p>Internship Program for Bioinformatics / Biotechnology Professionals Currently we offer positions to outstanding students interested in Next Generation Sequencing (NGS) data analysis. Applications are accepted throughout the year. Accepted students will be listed on web with their schedules. Accepted students can attend our future workshops and trainings freely at the specified venue.</p>

<p>Interested candidates may email their resume along with a cover letter to careers@arraygen.com</p>

<p>Official website: http://www.arraygen.com/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14215/the-8000-years-old-tibetian-gene-mutation</guid>
	<pubDate>Wed, 20 Aug 2014 21:57:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14215/the-8000-years-old-tibetian-gene-mutation</link>
	<title><![CDATA[The 8000 years old Tibetian gene mutation !!!]]></title>
	<description><![CDATA[<p>A new study has provided insight into how gene mutation around 8,000 years ago helped Tibetans' to survive in the thin air on the Tibetan Plateau, where an average elevation is of 14,800 feet.<br /><br />A study led by University of Utah scientists is the first to find a genetic cause for the adaptation, a single DNA base pair change that dates back 8,000 years and demonstrate how it contributes to the Tibetans' ability to live in low oxygen conditions.</p><p>About 8,000 years ago, the gene EGLN1 changed by a single DNA base pair. Today, a relatively short time later on the scale of human history, 88 percent of Tibetans have the genetic variation, and it was virtually absent from closely related lowland Asians. The findings indicate the genetic variation endows its carriers with an advantage.<br /><br />In those without the adaptation, low oxygen caused their blood to become thick with oxygen-carrying red blood cells, an attempt to feed starved tissues, which could cause long-term complications such as heart failure. The researchers found that the newly identified genetic variation protected Tibetans by decreasing the over-response to low oxygen.</p><p>Reference: http://www.nature.com/nature/journal/v512/n7513/abs/nature13408.html</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14024/grapher</guid>
	<pubDate>Thu, 14 Aug 2014 14:02:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14024/grapher</link>
	<title><![CDATA[GrapheR !!!]]></title>
	<description><![CDATA[<p>What a wonderful gem <em>GrapheR</em> is.... Oh yes it is. <em>GrapheR</em> is a GUI for base graphics in R by http://www.maximeherve.com/. The package provides a graphical user interface for creating base charts in R. It is ideal for beginners in R, as the user interface is very clear and the code is written along side into a text file, allowing users to recreate the charts directly in the console. <br /><br />Adding and changing legends? Messing around with the plotting window settings? It is much easier/quicker with this GUI than reading the help file and trying to understand the various parameters.<br />Here is a little example using the iris data set.<br /><br />library(GrapheR)<br />data(iris)<br />run.GrapheR()<br /><br />This will bring up a window that helps me to create the chart and tweak the various parameters.</p><p><img src="http://4.bp.blogspot.com/-NbnCM1dPh3E/U9aW9YxJ9oI/AAAAAAAABgo/gEPzPhOpf2Y/s1600/GrapheR.png" alt="image" width="878" height="868" style="border: 0px; border: 0px;"><br /><br />Finally, I find the underlying R code in a file created by <em>GrapheR</em>. For more details read also the <a href="http://cran.r-project.org/web/packages/GrapheR/index.html" target="_blank">package vignette</a>, which is available in <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_en.pdf" target="_blank">English</a>, <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_fr.pdf" target="_blank">French</a> and <a href="http://cran.r-project.org/web/packages/GrapheR/vignettes/manual_de.pdf" target="_blank">German</a>!</p>]]></description>
	<dc:creator>John Parker</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/14186/pybedtools</guid>
	<pubDate>Wed, 20 Aug 2014 01:03:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/14186/pybedtools</link>
	<title><![CDATA[pybedtools]]></title>
	<description><![CDATA[<p>pybedtools is a Python wrapper for Aaron Quinlan's BEDtools programs (https://github.com/arq5x/bedtools), which are widely used for genomic interval manipulation or "genome algebra". pybedtools extends BEDTools by offering feature-level manipulations from with Python. See full online documentation, including installation instructions, at http://pythonhosted.org/pybedtools/.</p><p>More at http://pythonhosted.org/pybedtools/</p><p>A powerful toolset for genome arithmetic.http://code.google.com/p/bedtools/</p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17515/ngs-online-training</guid>
  <pubDate>Sat, 27 Sep 2014 07:42:29 -0500</pubDate>
  <link></link>
  <title><![CDATA[NGS Online Training]]></title>
  <description><![CDATA[
<p>ArrayGen Technologies announces to provide online NGS training through out the globe. Now analyze your own NGS datasets from anywhere.For more information contact us at training@arraygen.com</p>

<p>Please visit our site at www.arraygen.com</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17966/internship-program-for-bioinformatics-biotechnology-professionals-no-of-vacancy-2</guid>
  <pubDate>Wed, 08 Oct 2014 01:10:08 -0500</pubDate>
  <link></link>
  <title><![CDATA[Internship Program for Bioinformatics / Biotechnology Professionals (No. Of Vacancy: 2)]]></title>
  <description><![CDATA[
<p>ArrayGen is offering an Internship Program for Post graduate Bioinformatics / Biotechnology students and professionals. ArrayGen Technologies provide an excellent opportunity to gain research experience and explore if a scientific career is right for you. Currently we offer positions to outstanding students interested in Next Generation Sequencing (NGS) data analysis. Applications are accepted throughout the year. Accepted students will be listed on web with their schedules. Accepted students can attend our future workshops and trainings freely at the specified venue.</p>
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